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AAGGAAAAGTCTTCAAAGAAAGGGA[A/G]GGGGAAAAAGAAGCAGTATCTATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138492 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLRB PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GLRB - glycine receptor beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000824.4 | 294 | Missense Mutation | AAG,AGG | K,R 31 | NP_000815.1 | |
NM_001166060.1 | 294 | Missense Mutation | AAG,AGG | K,R 31 | NP_001159532.1 | |
NM_001166061.1 | 294 | Missense Mutation | AAG,AGG | K,R 31 | NP_001159533.1 | |
XM_017008034.1 | 294 | Intron | XP_016863523.1 | |||
XM_017008035.1 | 294 | Missense Mutation | AAG,AGG | K,R 31 | XP_016863524.1 |